Sr. Pharmacovigilance Ops Specialist - Oncology Biotech

SystImmune, Inc.; Princeton (NJ); Híbrido; USD 85.000 - 115.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

100% paid medical/dental/vision

Short-term disability

Long-term disability

401(k) match

PTO 15 days

11 paid holidays

Descripción de la vacante

SystImmune, Inc. is seeking a PV Operations Specialist to support the Senior Director of Pharmacovigilance. You will oversee end-to-end safety case processing, ensure data integrity in the PV database, and coordinate regulatory submissions across global markets.

The role requires 3–5+ years in pharmacovigilance, a life sciences degree, and familiarity with safety databases such as ArisG or Argus. This hybrid position offers 3 days in-office and a comprehensive benefits package.

Formación

• Bachelor’s degree in life sciences, pharmacy, nursing, or related field.
• 3–5+ years of pharmacovigilance case processing experience preferred.
• Familiarity with safety databases (e.g., ArisG, Argus) and regulatory reporting requirements.
• Strong attention to detail, organizational skills, and ability to work independently.

Responsabilidades

• Perform intake, triage, data entry, and quality review of cases.
• Ensure timely regulatory submissions in accordance with global requirements.
• Maintain accuracy and completeness of safety data in the PV database.
• Collaborate with cross-functional teams to support audits, inspections, and CAPA implementation.
• Follow SOPs, work instructions, and applicable regulations (FDA, EMA, ICH).
• Support continuous improvement initiatives within PV operations.
• Facilitate generation of listings for periodic safety reports (DSUR, PSUR).
• Work with QA to maintain PV inspection readiness across regions.
• Support root cause analysis of PV-related deviations.
• Prepare responses to audit findings for PV department.
• Manage reconciliation activities with other departments and vendors.

Conocimientos

Pharmacovigilance

Attention to detail

Independent worker

Cross-functional collaboration

Educación

Bachelor’s degree in life sciences/related field

Herramientas

ArisG

Argus

Descripción del empleo

SystImmune is a leading and well-funded clinical-stage biopharmaceutical company located in Redmond, WA and Princeton, NJ. It specializes in developing innovative cancer treatments using its established drug development platforms, focusing on bi-specific, multi-specific antibodies, and antibody-drug conjugates (ADCs). SystImmune has multiple assets in various stages of clinical trials for solid tumor and hematologic indications. Alongside ongoing clinical trials. SystImmune has a robust preclinical pipeline of potential cancer therapeutics in the discover and IND-enabling stages, representing cutting-edge biologics development. We offer an opportunity for you to learn and grow while making significant contributions to the company's success.

The PV Operations Specialist supports the Senior Director of Pharmacovigilance (PV) Operations in the oversight and execution of Systimmune’s global pharmacovigilance function. The position carries full accountability for end-to-end safety case processing, including regulatory submissions, hands-on work within the safety database, and CAPA management and coordination.

The incumbent is responsible for ensuring data integrity, optimal system performance, and compliance with global pharmacovigilance regulations and internal SOPs. The role requires close cross-functional collaboration with internal stakeholders and effective partnership with external vendors and service providers on pharmacovigilance-related activities.

Hybrid position, requiring in-office presence a minimum of three days per week.

Key Responsibilities

• Perform intake, triage, data entry, and quality review of ISCrs.
• Ensure timely regulatory submissions in accordance with global requirements.
• Maintain accuracy and completeness of safety data in the PV database.
• Collaborate with cross-functional teams to support audits, inspections, and CAPA implementation.
• Follow SOPs, work instructions, and applicable regulations (e.g., FDA, EMA, ICH).
• Support continuous improvement initiatives within PV operations.
• Facilitate the generations of listings for the periodic safety reports (e.g., DSUR, PSUR).
• Work with the QA department to maintain a state of high PV inspection readiness across all regions/countries.
• Support the performance of root cause analysis of deviations relevant to PV systems.
• Prepare responses to audit findings that concern the PV department.
• Manage reconciliation activities with other departments within the company and vendors.

Qualifications

• Bachelor’s degree in life sciences, pharmacy, nursing, or related field.
• 3-5+ years of experience in pharmacovigilance case processing preferred.
• Familiarity with safety databases (e.g., ArisG, Argus) and regulatory reporting requirements.
• Strong attention to detail, organizational skills, and ability to work independently.

Compensation and Benefits:

The expected base salary range for this position is $85,000 - $115,000annually. Actual compensation will be based on a variety of factors, including but not limited to a candidate’s level qualifications, experience, and skills.

SystImmune is a leading and well-funded biotech company with a bright future. We offer an opportunity for you to learn and grow while making significant contributions to the company’s success. SystImmune offers a comprehensive benefits package including: 100% paid employee premiums for medical/dental/vision, also STD, LTD, a 401(k) plan with a 50% company match of up to 3% and a vesting schedule of only 5 years, 15 PTO days per year, sick leave, plus 11 paid holidays and MORE.

We offer an opportunity for you to learn and grow while making significant contributions to the company’s success.

SystImmune is an Equal Opportunity Employer. We welcome diverse talent and encourage all qualified applicants to apply.